Coronavirus Vaccine Recipients Suddenly Test Positive For HIV (Figures as HIV Was Attached to This COVID Virus in a Bioweapons Lab-Wuhan) & FDA Approves This Vaccine!
DEPOPULATION VAX: Trial subjects injected with coronavirus vaccines suddenly test positive for HIV – updated
Friday, December 11, 2020 by: Mike Adams
Tags: badhealth, badmedicine, badscience, Big Pharma, bioweapons, coronavirus, covid-19, depopulation, HIV, medical experiments, outbreak, pandemic, vaccines
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(Natural News) The coronavirus vaccine is a global depopulation bioweapon. People injected with covid-19 vaccines are suddenly testing positive for HIV.
As reported via Great Game India:
Australia Scraps Billion Dollar Coronavirus Vaccine After Participants Test HIV Positive
The Australian Government has scrapped a billion dollar coronavirus vaccine agreement with Australian biotech company CSL Limited to supply 51 million doses of a Covid-19 vaccine being developed by the University of Queensland after several trial participants returned false positive HIV test results.
What’s interesting is that this story is claiming the HIV tests are “false positives.” But if HIV is actually detected, then how is it false?
Notice that when someone is found to be carrying the coronavirus, it’s never called a false positive. It’s simply called a “positive” result or a new “case” of infection. By that logic, these vaccine recipients should also be labeled “cases” of HIV.
And it begs the question: What’s being put into the vaccine that resembles HIV closely enough to trigger a positive test result?
HIV protein fragments intentionally added to coronavirus vaccines
From the story linked above:
Mr Petrovsky told The Australian the problem with the use of HIV was clear in the ‘hamster and mouse data’ but his advice was ignored. He said the early data suggested the vaccine itself was quite unstable.
Covid’s spike proteins, like most surface viral proteins, are fairly unstable. To ensure that the vaccine induced the right immune response, the clamp chosen comprises two fragments of a protein found in HIV, as those fragments provided the greatest stability to the vaccine.
So wait, they’re using HIV components in the vaccine on purpose?
Indeed, yes.
And this is why it’s triggering the HIV “positive” test results. In other words, they aren’t false positives at all. They’re detecting the HIV components that are being deliberately put into the coronavirus vaccine.
Technically, it would be accurate to state that the coronavirus vaccine is using “HIV protein fragments” as a deliberate component of the vaccine.
So people who are lining up to be injected with the coronavirus vaccine may be volunteering to be injected with HIV protein fragments.
But anyone who mentions this will of course be instantly deplatformed on all the social media platforms, even when it’s 100% true.
It should be readily apparent to any rational person that the coronavirus vaccine is a global depopulation bioweapon that’s designed to injure, kill or make infertile billions of human beings.
Anyone who takes the coronavirus vaccine is begging for vaccine-assisted suicide.
Unless, of course, you are suicidal.
An earlier version of this story reported that Robert F. Kennedy, Jr. had issued a warning that no one should take the covid-19 vaccine. Bobby Kennedy’s representatives reached out and informed us this was not accurate, so we retracted that statement. We are researching that claim, which appears to be widely reported by other media outlets, but may be incorrect nonetheless. We regret the error.Previous :Situation Update, Dec. 10th – Texas lawsuit with SCOTUS reveals pathway to instant victory for TrumpNext :Situation Update, Dec. 11th – DoD de-fangs the CIA, 305th intel proves foreign interference, SCOTUS maneuvers14KVIEWS
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About the author: Mike Adams (aka the “Health Ranger“) is a best selling author (#1 best selling science book on Amazon.com called “Food Forensics“), an environmental scientist, a patent holder for a cesium radioactive isotope elimination invention, a multiple award winner for outstanding journalism, a science news publisher and influential commentator on topics ranging from science and medicine to culture and politics. Follow his videos, podcasts, websites and science projects at the links below.
Mike Adams serves as the founding editor of NaturalNews.com and the lab science director of an internationally accredited (ISO 17025) analytical laboratory known as CWC Labs. There, he was awarded a Certificate of Excellence for achieving extremely high accuracy in the analysis of toxic elements in unknown water samples using ICP-MS instrumentation. Adams is also highly proficient in running liquid chromatography, ion chromatography and mass spectrometry time-of-flight analytical instrumentation. He has also achieved numerous laboratory breakthroughs in the programming of automated liquid handling robots for sample preparation and external standards prep.
The U.S. patent office has awarded Mike Adams patent NO. US 9526751 B2 for the invention of “Cesium Eliminator,” a lifesaving invention that removes up to 95% of radioactive cesium from the human digestive tract. Adams has pledged to donate full patent licensing rights to any state or national government that needs to manufacture the product to save human lives in the aftermath of a nuclear accident, disaster, act of war or act of terrorism. He has also stockpiled 10,000 kg of raw material to manufacture Cesium Eliminator in a Texas warehouse, and plans to donate the finished product to help save lives in Texas when the next nuclear event occurs. No independent scientist in the world has done more research on the removal of radioactive elements from the human digestive tract.
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FDA panel votes in favor of Pfizer COVID-19 vaccine
BY NATHANIEL WEIXEL – 12/10/20 05:39 PM EST 8,714923
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A federal panel of outside experts on Thursday endorsed a coronavirus vaccine from Pfizer and BioNTech, and recommended the Food and Drug Administration (FDA) move forward with emergency authorization.
The panel voted 17-4, with one abstention, that the safety and efficacy of the vaccine outweigh the risks for use in individuals age 16 and older.
The vote is an important step, as the country is poised to start an unprecedented vaccination campaign to stop the COVID-19 pandemic.
FDA doesn’t necessarily have to follow the panel’s recommendation, but it’s widely expected to do so.
Peter Marks, the director of the FDA division overseeing vaccines, said Wednesday that a decision would come “days to a week” after the advisory panel meeting.
Once FDA gives the official green light, the administration plans to start shipping millions of doses to states across the country. Operation Warp Speed, the White House initiative to develop and distribute vaccines, has said it plans to begin shipping the vaccine within 24 hours.
The final step before shots can go into arms is a Centers for Disease Control and Prevention (CDC) vaccine advisory panel. An emergency meeting has been scheduled for Sunday. Once that panel gives the OK, vaccinations can start.
The FDA tipped its hand on a decision earlier this week, when reviewers on Tuesday endorsed the safety and effectiveness of the vaccine, finding it was 95 percent effective at preventing infection after two doses.
These findings were consistent across subgroups in the 44,000 person trial. The trial included people older than 65, people of various ethnicities, as well as people with other health conditions such as obesity, diabetes, hypertension and chronic cardiopulmonary disease.
The unprecedented demand for the public meeting led FDA to host it on YouTube. The commitment to transparency is key for the agency, as it needs to convince the public that the vaccine developed in record time is safe.
The U.S. needs to vaccinate close to 70 percent of the population to achieve herd immunity, and it’s going to take time, even if the vaccine is widely accepted.
Officials like Anthony Fauci, the country’s top infectious diseases doctor, don’t expect the majority of the population to get vaccinated until next spring or summer.
In the meantime, the death toll is going to rise. More than 3,000 people died Wednesday, and CDC Director Robert Redfield said the upcoming months are going to be brutal.
“The reality is the vaccine approval this week’s not going to really impact that I think to any degree for the next 60 days,” Redfield said Thursday. “We are in the timeframe now that probably for the next 60 to 90 days we’re going to have more deaths per day than we had at 9/11 or we had at Pearl Harbor.”
While there was evidence of protection after just one dose of the vaccine, Pfizer executives and FDA officials at the meeting emphasized there isn’t enough evidence to conclude a single dose of this vaccine would give the same long-term protection.
The Hill Special Report: America’s Most Reliable Voter
BY AARP
According to FDA, the main benefit of the vaccine is a reduced risk of COVID-19 at least seven days after completion of the second dose.
However, the data is limited as to just how much protection the vaccine gives. The vaccine technology is completely untested in humans, and the trials only have data from a couple months.
FDA’s Dorian Fink noted that there are plenty of examples of vaccines that protect just as well against severe disease as they do against mild to moderate, and protection against disease of any severity is a “pretty good predictor” of what it means for severe disease.
Still, neither FDA nor Pfizer has a large amount of evidence to show that the vaccine can protect against severe disease, or even how long protection lasts.
Data on how well the vaccine protects against asymptomatic infection is expected early next year.
Some committee members expressed concern that they were voting on recommending the vaccine for people as young as 16, even though they had limited evidence, which is what led to some of the “no” votes.
Panel member Paul Offit, director of the Vaccine Education Center at Children’s Hospital of Philadelphia, said that sometimes decisions have to be made without knowing all the evidence
“It’s not a question of when do you know everything, but when do you know enough?” Offit said. “We have clear evidence of benefit but only theoretical risk.”TAGS PFIZERSTEPHEN HAHNANTHONY FAUCIROBERT REDFIELDCORONAVIRUSVACCINECOVID-19FOOD AND DRUG ADMINISTRATION LOAD TEXT COMMENTS (8,714)LOAD VIDEO COMMENTS